A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999379



Internal ID19158915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80344838..80378161hg38UCSC Ensembl
Innerchr1:80810523..80843846hg19UCSC Ensembl
Innerchr1:80583111..80616434hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3833324
hg1933324
hg1833324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3480133
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer